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Full-time
postgraduate degree
Competitive Compensation, Career Development Opportunities
Posted 20d ago
~40 hrs/week
Responsibilities
Lead the Global Cluster Regulatory organization to provide senior leadership for in-market regulatory strategy, registration delivery, and launch readiness. Act as the senior regulatory partner to commercial leadership to ensure compliant growth and supply continuity across clusters.
Requirements
Requires an advanced degree in Life Sciences or Pharmacy and over 15 years of progressive regulatory affairs experience, including global leadership roles. Must demonstrate a blend of technical expertise with commercial acumen and experience leading matrixed, geographically dispersed teams.
Full job description
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to win in self-care.
Description Overview
We are excited to recruit a Vice President, Head of Regulatory Affairs – Cluster. In this role you will lead the Global Cluster Regulatory organisation and provide senior leadership for in-market regulatory strategy, execution, registration delivery, launch readiness, lifecycle transition and ongoing market support.
This role is the senior regulatory partner to Cluster and Commercial Leadership, translating global regulatory intent into clear local execution that supports business performance, market access, supply continuity and compliant growth.
Your role is accountable for cluster regulatory strategies, national registrations, health authority interactions, labelling and promotional compliance, submission quality, approval, timing, launch readiness, post-approval execution and issue escalation.
As VP, you will define the operating model, decision rights, governance and escalation pathways needed to connect Category Regulatory Affairs, Cluster Regulatory Affairs, Lifecycle Management, Regulatory Operations, Quality, Safety, Supply, R&D and Commercial teams into one execution-focused regulatory voice.
Where required, the role may also directly lead one cluster. In that case, as a VP you must maintain clear separation between enterprise leadership and cluster execution, with transparent prioritization, delegation and escalation.
Scope of the Role
Cluster Regulatory Strategy, Execution and Business Partnership
Define and lead cluster regulatory strategy, translating global regulatory intent into executable market plans aligned to category strategy, commercial priorities and enterprise value creation
Provide VP-level leadership for registration execution, launch delivery, market access, supply continuity, regulatory risk management and prioritisation across clusters
Act as the senior regulatory partner to Cluster Commercial Leadership, providing clear options, risks, recommendations and decision support for growth, launch and portfolio decisions
In-Market Regulatory Delivery and Lifecycle Management
Lead regulatory delivery from global strategy handover through local submission, approval, launch, post-approval execution and ongoing in-market support
Ensure high-quality, timely and compliant submissions, authority interactions, approvals, labelling, artwork and launch readiness across relevant product classifications
Ensure effective transition into lifecycle management, including post-approval commitments, variations, renewals, compliance actions and market-specific maintenance requirements
Health Authority Engagement, Governance and Risk Management
Act as the senior regulatory representative with health authorities, regulatory bodies, industry associations and external forums across clusters
Lead senior-level escalation, negotiation and issue management where regulatory matters may affect approval timing, supply continuity, claims, compliance position or business value
Establish governance, metrics and prioritisation to ensure visibility of workload, delivery, risks, dependencies and resource capacity
Ensure regulatory compliance, inspection readiness, audit preparedness and effective mitigation of in-market regulatory risks
Cross-Pillar Integration and Operating Model
Partner with Category RA, Lifecycle Management, Regulatory Operations, Quality, Safety, Supply, R&D and Commercial teams to ensure strategies, dossiers, claims, hand-offs and execution plans are clear and aligned
Define decision rights, ownership, escalation routes and ways of working that enable a single regulatory voice across markets
Drive cross-pillar prioritisation, transparency and resolution of execution challenges through established governance forums
Leadership and Capability Building
Shape and lead the global Cluster Regulatory organisation, ensuring structure, roles, capabilities and resources align with market needs, portfolio priorities and future business requirements
Build capability in cluster regulatory strategy, in-market execution, authority engagement, commercial partnering and lifecycle delivery
Lead and develop Cluster Regulatory Leads, including performance management, succession planning, capability development and delivery accountability
Where applicable, directly lead one cluster alongside VP responsibilities, with clear delegation, decision rights and prioritisation so enterprise leadership remains effective
Experience Required
Advanced degree in Life Sciences, Pharmacy, or related field.
15+ years of progressive regulatory affairs experience, including cluster or global leadership roles.
Demonstrated ability to blend technical expertise with commercial, strategic business priorities. Experience within Consumer Healthcare would be a distinct advantage.
Proven experience in cluster regulatory strategy, in-market execution, submissions, approvals, health authority interactions and lifecycle delivery across multiple markets.
Strong track record of delivering regulatory outcomes that support commercial performance and market access.
Demonstrated ability to operate at VP level while also providing hands-on cluster leadership when required.
Experience leading global, matrixed, and geographically dispersed teams.
Experienced strategic cluster leader with demonstrated execution excellence.
Regulatory expertise and risk-based decision-making are core to success in this role.
You bring strong commercial acumen and business partnership, along with demonstrated ability to influence internal and external stakeholders.
Cross-functional and cross-pillar collaboration.
Leadership and organisational capability building.
Ability to balance enterprise VP leadership with direct cluster accountability where required.
Benefits We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Hybrid Working Approach We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.
We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here
Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo
We are driven by our mission to Make Lives Better Through Trusted Health and Wellness Solutions, Accessible to All.
Industry
Manufacturing
Company size
5,001-10,000 employees
Headquarters
Dublin, County Dublin
LinkedIn followers
112,557
Total funding
$4.6B
Perrigo is a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula.
We are driven by our mission to Make Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, ACO®, and many more.
Offices: 10-12 Hogan Place, The Sharp Building, Dublin, County Dublin, IE · 515 Eastern Ave, Allegan, MI 49010, US · Nazareth, 9810, BE · Vienna, AT · Paris, FR
How many Science & Research jobs are open in Zurich, Switzerland right now?
There are currently 269 open science & research positions in Zurich, Switzerland listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Zurich, Switzerland?
Companies currently hiring include NEURA Robotics, Takeda, Destinus, Google, Mediclinic Middle East, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Zurich, Switzerland?
Yes — 88 of the 269 open science & research positions offer remote or hybrid work (19 remote, 69 hybrid).
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